Canonical Allele Identifier: CA2816661567

Gene: SALL4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784785_51784786insAC , CM000682.2:g.51784785_51784786insAC	GRCh38
NC_000020.10:g.50401324_50401325insAC , CM000682.1:g.50401324_50401325insAC	GRCh37
NC_000020.9:g.49834731_49834732insAC	NCBI36
NG_008000.1:g.22724_22725insGT , LRG_675:g.22724_22725insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217086.9:c.2743-102_2743-101insGT MANE Select	ENSP00000217086.4:n.2743-102_2743-101insGT
ENST00000217086.8:c.2743-102_2743-101insGT	ENSP00000217086.4:n.2743-102_2743-101insGT
ENST00000371539.7:c.412-102_412-101insGT	ENSP00000360594.3:n.412-102_412-101insGT
ENST00000395997.3:c.1432-102_1432-101insGT	ENSP00000379319.3:n.1432-102_1432-101insGT
NM_020436.3:c.2743-102_2743-101insGT , LRG_675t1:c.2743-102_2743-101insGT	NP_065169.1:n.2743-102_2743-101insGT
XM_005260467.2:c.2437-102_2437-101insGT	XP_005260524.1:n.2437-102_2437-101insGT
XM_006723834.2:c.2437-102_2437-101insGT	XP_006723897.1:n.2437-102_2437-101insGT
XM_011528919.1:c.2617-102_2617-101insGT	XP_011527221.1:n.2617-102_2617-101insGT
XM_011528920.1:c.2437-102_2437-101insGT	XP_011527222.1:n.2437-102_2437-101insGT
XM_011528921.1:c.2437-102_2437-101insGT	XP_011527223.1:n.2437-102_2437-101insGT
XM_011528922.1:c.2437-102_2437-101insGT	XP_011527224.1:n.2437-102_2437-101insGT
XM_011528923.1:c.1432-102_1432-101insGT	XP_011527225.1:n.1432-102_1432-101insGT
NM_001318031.1:c.1432-102_1432-101insGT	NP_001304960.1:n.1432-102_1432-101insGT
NM_020436.4:c.2743-102_2743-101insGT	NP_065169.1:n.2743-102_2743-101insGT
XM_005260467.4:c.2437-102_2437-101insGT	XP_005260524.1:n.2437-102_2437-101insGT
XM_011528921.2:c.2437-102_2437-101insGT	XP_011527223.1:n.2437-102_2437-101insGT
XM_011528922.2:c.2437-102_2437-101insGT	XP_011527224.1:n.2437-102_2437-101insGT
NM_020436.5:c.2743-102_2743-101insGT MANE Select	NP_065169.1:n.2743-102_2743-101insGT
NM_001318031.2:c.1432-102_1432-101insGT	NP_001304960.1:n.1432-102_1432-101insGT